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Caseview

FDA UDI

Class I (US FDA UDI)

by PHYSIO-CONTROL, Inc.

Identity

Trade Name
Caseview FDA UDI
Generic Name
Medical equipment clinical data interfacing software FDA UDI
Device Name
SOFTWARE, CODE-STAT CASEVIEW SOFTWARE INSTALL FDA UDI
Model / Reference
21340 FDA UDI
Description
SOFTWARE, CODE-STAT CASEVIEW SOFTWARE INSTALL FDA UDI

Identifiers

Catalog Number
21340-000850 FDA UDI
Primary DI / UDI-DI
00883873837788 FDA UDI
FDA Product Code
OUG FDA UDI
GMDN Term
Medical equipment clinical data interfacing software FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6310 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Medical equipment clinical data interfacing software

Caseview by PHYSIO-CONTROL, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical equipment clinical data interfacing software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
PHYSIO-CONTROL, Inc.

Sources (1)

  • FDA UDI 96ddf5ec-4d18-416a-af88-6b97a7d27898 35 fields · synced Jun 9, 2026